ISO 13485  Medical Devices

Safety and quality are non-negotiable in the medical devices industry, and that is why we run an ISO 13485 Quality Management System.

Regulatory requirements are increasingly stringent throughout every step of a product’s life cycle, and ISO 13485 is a great way for us to show our commitment to ensuring that all of our design, manufacture and servicing processes are fully aligned with the very best practices of the medical device industry.